spinocerebellar ataxia 13

Preferred Label : spinocerebellar ataxia 13;

MeSH synonym : cerebellar ataxia, autosomal dominant with mental retardation; autosomal dominant cerebellar ataxia with mental retardation; SCA13 Spinocerebellar ataxia 13;

Details

Origin ID

C537195;

UMLS CUI

C1854488;

CISMeF manual mappings
- Spinocerebellar ataxia type 13 [ORDO Disease]
Currated CISMeF NLP mapping
- Spinocerebellar ataxia 13 [OMIM Phenotype]
- Spinocerebellar ataxia type 13 [ICD-11 More detail]
- Spinocerebellar ataxia type 13 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 13 [Disease (Nov.)]
- spinocerebellar ataxia type 13 [DO Concept]
MeSH term(s) associated for indexing
- spinocerebellar ataxias [MeSH Descriptor]
- spinocerebellar degenerations [MeSH Descriptor]
ORDO relation(s)
- Spinocerebellar ataxia type 13 [ORDO Disease]
Record concept(s)
- Spinocerebellar ataxia 13 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinocerebellar ataxia 13 [OMIM Phenotype]
- Spinocerebellar ataxia type 13 [ORDO Disease]
- Spinocerebellar ataxia type 13 [ICD-11 More detail]
- Spinocerebellar ataxia type 13 (disorder) [SNOMED CT concept]
- spinocerebellar ataxia 13 [Disease (Nov.)]
- spinocerebellar ataxia type 13 [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

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